- Trials with a EudraCT protocol (76)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (22)
76 result(s) found for: Rubella vaccine.
Displaying page 1 of 4.
EudraCT Number: 2011-005882-19 | Sponsor Protocol Number: 109995 | Start Date*: 2015-06-25 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: Non-inferiority of GSK Biologicals’ measles-mumps-rubella-varicella (MMRV) vaccine 208136 vs Priorix™ and Priorix™ coadministered with Varilrix™ (comparator) and to evaluate non-inferiority of Prio... | ||
Medical condition: Measles, mumps, rubella and varicella diseases | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-003672-36 | Sponsor Protocol Number: 115231,MMR159 | Start Date*: 2014-10-09 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals S.A. | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase IIIA, observer-blind, randomized study to evaluate non-inferiority of a second dose of GSK Biologicals’ measles-mumps-rubella vaccine vs. a second dose of Merck & Co., Inc.’s MMR vaccine wh... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Healthy volunteers (Active immunization against measles, mumps and rubella diseases of healthy subjects, 7 years of age and older). | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Children, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: SK (Completed) EE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-004371-11 | Sponsor Protocol Number: 103388 & 104690 | Start Date*: 2005-07-12 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase IIIB, partially blind, randomized study to evaluate the immunogenicity and safety of GlaxoSmithKline Biologicals’ measles-mumps-rubella-varicella vaccine (MeMuRu-OKA) given to healthy child... | ||
Medical condition: Active immunization of healthy children during their second year of life against measles, mumps, rubella and varicella diseases. | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004638-32 | Sponsor Protocol Number: 115158 | Start Date*: 2015-06-11 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase IIIA, observer-blind, randomized study to evaluate non-inferiority of a second dose of GSK Biologicals’ measles-mumps-rubella vaccine vs. a second dose of Merck & Co., Inc.’s MMR vaccine wh... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Healthy volunteers (Active immunization against measles, mumps and rubella diseases of healthy subjects, 4 to 6 years of age). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004905-26 | Sponsor Protocol Number: 115649 | Start Date*: 2012-10-10 | ||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||||||||||||
Full Title: Immunogenicity and safety study of GSK Biologicals’ Priorix® vaccine (209762) at an end of shelf-life potency compared to Merck & Co., Inc.’s MMR vaccine when both are given on a 2-dose schedule to... | ||||||||||||||||||||||||||||
Medical condition: Healthy volunteers (Active immunization against measles, mumps and rubella diseases of healthy children in their second year of life). | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) CZ (Completed) ES (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-005263-19 | Sponsor Protocol Number: 104389 | Start Date*: 2005-05-03 |
Sponsor Name:GSK Biologicals | ||
Full Title: A phase III, blinded, randomised, controlled study to evaluate the immunogenicity and safety of three production lots of GlaxoSmithKline Biologicals’ combined measles-mumps-rubella-varicella (MeMuR... | ||
Medical condition: Active immunization of healthy children during their second year of life against measles, mumps, rubella and varicella diseases. | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004485-15 | Sponsor Protocol Number: 110876 | Start Date*: 2015-06-25 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A Phase IIIb, open, randomized study to evaluate non-inferiority of GSK Biologicals’ measles-mumps-rubella-varicella vaccine versus co-administration of GSK Biologicals’ Priorix™ and Varilrix™ in h... | ||
Medical condition: Measles, mumps, rubella and varicella diseases | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-005881-38 | Sponsor Protocol Number: 108760 | Start Date*: 2015-06-25 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase II, randomized, double-blind study of Priorix-Tetra (combined measles-mumps-rubella-varicella vaccine), one lot using new measles and rubella working seeds and one lot using old working see... | ||
Medical condition: Measles, mumps, rubella and varicella diseases | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-006161-18 | Sponsor Protocol Number: 115650 | Start Date*: 2014-09-25 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A phase IIIA, randomized, observer-blind, controlled, multinational study to evaluate the safety and immunogenicity of GSK Biologicals' MMR vaccine (209762) (Priorix®) compared to Merck & Co., Inc.... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Healthy volunteers (Active immunization against measles, mumps and rubella diseases in healthy children, 12 to 15 months of age) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: EE (Completed) FI (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004891-12 | Sponsor Protocol Number: 115648 | Start Date*: 2012-11-02 | ||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||||||||||||
Full Title: A phase IIIA, randomized, observer-blind, controlled, multinational consistency study to evaluate the immunogenicity and safety of GSK Biologicals' MMR vaccine (209762) (Priorix®) compared to Merck... | ||||||||||||||||||||||||||||
Medical condition: Healthy volunteers (Active immunization against measles, mumps and rubella diseases of healthy children in their second year of life). | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: EE (Completed) FI (Completed) ES (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001608-37 | Sponsor Protocol Number: 115555MMRV-063 | Start Date*: 2011-12-16 | ||||||||||||||||||||||||||
Sponsor Name:GLAXOSMITHKLINE BIOLOGICALS SA | ||||||||||||||||||||||||||||
Full Title: Open, randomised, controlled, multicenter Phase IIIb study to evaluate the immune response and safety, after the administration of GlaxoSmithKline Biologicals live attenuated measles mumps rubell... | ||||||||||||||||||||||||||||
Medical condition: Vaccination of children from the age of 9 months up to 12 years inclusive against measles, mumps, rubella and varicella diseases | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005860-31 | Sponsor Protocol Number: 111870 | Start Date*: 2015-06-25 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: Immunogenicity of GlaxoSmithKline Biologicals’ MMR vaccine (209762) vs. M-M-R® II, when co-administered with hepatitis A, varicella and pneumococcal conjugate vaccines to children 12-15 months of age | ||
Medical condition: Diseases caused by measles, mumps, rubella and varicella viruses | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2017-000454-18 | Sponsor Protocol Number: 110058 | Start Date*: 2017-07-10 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A Phase II randomized, observer blind, multicenter study of GlaxoSmithKline (GSK) Biologicals’ combined measles-mumps-rubella-varicella vaccine (MMRV) versus ProQuad, according to a one dose schedu... | ||
Medical condition: Healthy volunteers (Use of the candidate MMRV vaccine for immunization of healthy children 12 - 14 months of age against measles, mumps, rubella and varicella). | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2005-005944-22 | Sponsor Protocol Number: 106670 | Start Date*: 2006-02-21 |
Sponsor Name:GlaxoSmithKline GmbH & Co. KG | ||
Full Title: Open, multicenter, randomised, controlled phase IIIb study evaluating the immunogenicity and safety of subcutaneous versus intramuscular administration of GlaxoSmithKline Biologicals’ combined meas... | ||
Medical condition: Active immunization of healthy children aged 11 to 21 months against measles, mumps, rebella and varicella diseases | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003318-81 | Sponsor Protocol Number: 111846 | Start Date*: 2008-11-17 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase IV, open, randomized, controlled study to demonstrate the non-inferiority of co-administration of GSK Biologicals’ live attenuated measles-mumps-rubella-varicella vaccine and Baxter’s Neiss... | ||
Medical condition: Active immunization of healthy children during their second year of life against measles, mumps, rubella, varicella and Neisseria meningitidis C diseases | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-002586-21 | Sponsor Protocol Number: X04-MMRr-301 | Start Date*: 2004-12-23 |
Sponsor Name:Aventis Pasteur MSD SNC | ||
Full Title: An open, randomised, comparative, multicentre study of the immunogenicity and safety of M-M-R™II manufactured with recombinant Human Albumin (rHA) and VARIVAX® when administered concomitantly by in... | ||
Medical condition: Not applicable - Healthy subjects | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-006065-14 | Sponsor Protocol Number: 105908 | Start Date*: 2006-04-04 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase II, open, randomised, comparative study to evaluate the immunogenicity and safety of GlaxoSmithKline's (GSK) Biologicals' measles-mumps-rubella-varicella candidate vaccine (MeMuRu-OKA) and ... | ||
Medical condition: Healthy male and female children between 15 months and 6 years of age who previously received an MMR vaccine will receive one dose of MMR + V or MMRV. A second dose of varicella vaccine will be giv... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004129-27 | Sponsor Protocol Number: X06-MMRV-302 | Start Date*: 2006-12-13 |
Sponsor Name:Sanofi Pasteur MSD | ||
Full Title: An open, randomised, comparative, multicentre study of the immunogenicity and safety of concomitant versus separate administration of a combined measles, mumps, rubella and varicella live vaccine (... | ||
Medical condition: The study will involve healthy children. | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002676-41 | Sponsor Protocol Number: 100388,103494,104105,104106 | Start Date*: 2005-05-23 | ||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||||||||||||
Full Title: Blinded, randomised, controlled, multicenter study to evaluate the clinical efficacy against varicella disease of GlaxoSmithKline Biologicals’ live attenuated varicella vaccine (Varilrix) given on ... | ||||||||||||||||||||||||||||
Medical condition: Healthy children between 12-22 months (including the day before the 23-month birthday) of age at the time of vaccination with no history of measles, mumps, rubella and varicella diseases/vaccination. | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Completed) LT (Completed) SK (Completed) CZ (Completed) IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002468-88 | Sponsor Protocol Number: MRV02C | Start Date*: 2007-10-12 |
Sponsor Name:Sanofi Pasteur MSD SNC | ||
Full Title: An open-label, randomised, comparative, multi-centre study of the immunogenicity and safety of a 2-dose regimen of ProQuad® manufactured with rHA administered to healthy children from 9 months of age | ||
Medical condition: Measles, mumps, rubella and varicella vaccine administered to healthy children from 9 months of age | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) DE (Completed) FI (Completed) | ||
Trial results: View results |
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